Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)

Chromosome 22:21031579 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2504 sample genotypes.

Variant displays